JP3113454B2 - Artificial knee joint - Google Patents
Artificial knee jointInfo
- Publication number
- JP3113454B2 JP3113454B2 JP13036193A JP13036193A JP3113454B2 JP 3113454 B2 JP3113454 B2 JP 3113454B2 JP 13036193 A JP13036193 A JP 13036193A JP 13036193 A JP13036193 A JP 13036193A JP 3113454 B2 JP3113454 B2 JP 3113454B2
- Authority
- JP
- Japan
- Prior art keywords
- femur
- femoral
- side member
- resection
- wall
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 210000000629 knee joint Anatomy 0.000 title claims description 16
- 210000000689 upper leg Anatomy 0.000 claims description 40
- 210000000988 bone and bone Anatomy 0.000 claims description 19
- 238000002271 resection Methods 0.000 description 23
- 239000002639 bone cement Substances 0.000 description 3
- 210000003127 knee Anatomy 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 210000002303 tibia Anatomy 0.000 description 2
- 208000006386 Bone Resorption Diseases 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000024279 bone resorption Effects 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 210000003041 ligament Anatomy 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 201000008482 osteoarthritis Diseases 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000011883 total knee arthroplasty Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/38—Joints for elbows or knees
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
Landscapes
- Health & Medical Sciences (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Prostheses (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、変形性関節症などの疾
患により機能が著しく低下もしくは喪失し、疼痛の増大
した膝関節を置換する、人工膝関節に関するものであ
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an artificial knee joint for replacing a knee joint whose function has been significantly reduced or lost due to a disease such as osteoarthritis and pain has increased.
【0002】[0002]
【従来の技術】人工膝関節置換術において、大腿骨側部
材が大腿骨に強固に固定されるためには、前壁と後壁の
内面とこれに当接する大腿骨遠位部関節面の骨切り面
を、大腿骨側部材を大腿骨遠位部に打ち込む際に適度な
圧入力が得られるように、骨との間に適度な圧入しろを
確保するよう、精度よく行うことが必要であった。2. Description of the Related Art In a total knee arthroplasty, in order for a femoral side member to be firmly fixed to a femur, the bones on the inner surfaces of anterior wall and posterior wall and the distal joint surface of the femur contacting the inner surfaces of the anterior wall and the posterior wall. It is necessary to accurately perform the cut surface so as to obtain an appropriate press-fit between the bone and the bone so that an appropriate press-fit is obtained when the femoral side member is driven into the distal portion of the femur. Was.
【0003】しかし、現実の骨切り精度はこれに見合う
程十分なものではなく、面と面の多少のずれや隙間の発
生は止むを得ない事である。例えば、骨切りの角度を5
°とすると、通常の骨切り器具では、角度にして1°〜
2°程度のばらつきが発生する。それ故、骨と大腿骨側
部材との間に隙間が生じ、大腿骨部材をしっかり固定で
きなかったり、逆に圧入しろが多すぎ、過度の圧入力で
大腿骨部材を固定したことにより大腿骨部材との当接面
付近の骨が過度に圧縮され、その結果、応力伝達が偏る
ようになり、所謂ストレスシールドなる、骨吸収を引き
起こしかねない状態になることもあった。大腿骨側部材
が金属材料より構成されているならば、このような場合
であっても、前壁や後壁が比較的容易に弾性変形し、こ
れによって固定後初期に骨切りによるずれを多少吸収す
ることができが、大腿骨側部材がセラミックスのような
脆性材料から構成されている時は、大腿骨との固定力を
骨切りの精度に依存しなければならず、もし、精度がな
い場合であれば骨セメントの使用を余儀なくされた。こ
のような骨切りにおける正確性が大きな問題であった。However, the actual osteotomy accuracy is not enough to match this, and it is inevitable that some deviations and gaps between surfaces occur. For example, if the osteotomy angle is 5
°, with a normal osteotomy device, the angle is 1 ° ~
A variation of about 2 ° occurs. Therefore, a gap is generated between the bone and the femur side member, and the femoral member cannot be fixed firmly, or conversely, there is too much press-fit, and the femoral member is fixed by excessive press-fitting. The bone near the contact surface with the member is excessively compressed, and as a result, the stress transmission is biased, which may be a so-called stress shield, which may cause bone resorption. If the femoral side member is made of a metal material, even in such a case, the anterior wall and the posterior wall are relatively easily elastically deformed. Although it can be absorbed, when the femur side member is made of a brittle material such as ceramics, the fixing force with the femur must depend on the accuracy of the osteotomy, and if there is no accuracy In some cases, the use of bone cement was forced. Accuracy in such osteotomy has been a major problem.
【0004】このような問題を解決する目的で設計され
た従来の人工膝関節として、特開昭63−279838
号公報に提案されているように、大腿骨側部材がその前
壁と後壁の内面で大腿骨遠位部を挟み込むように嵌合す
るように構成されるとともに、大腿骨遠位端面に当接す
る摺動部の内面に釘が形成し、この釘を大腿骨内に圧入
することにより、骨セメントを用いずに大腿骨に固定す
る人工膝関節があった。また、特開昭64−68255
号公報に提案されているように、上記釘の替わりに板状
のフィンを上記摺動部の内面に形成し、この板状フィン
を大腿骨内に圧入するよう構成するとともに、上記前壁
及び後壁の内面に、高さ1mm程度で鋸歯形状をなす複
数の歯状突起を形成し、大腿骨への固定力を高めるよう
工夫した大腿骨側部材を含む人工膝関節があった。A conventional artificial knee joint designed to solve such a problem is disclosed in Japanese Patent Application Laid-Open No. 63-279838.
As proposed in the publication, the femur side member is configured to fit so that the distal part of the femur is sandwiched between the inner surfaces of the anterior wall and the posterior wall, and the femoral side member contacts the distal end surface of the femur. There was an artificial knee joint in which a nail was formed on the inner surface of the sliding part in contact with the nail, and this nail was pressed into the femur to fix it to the femur without using bone cement. Further, Japanese Patent Application Laid-Open No. 64-68255
As proposed in the publication, a plate-shaped fin is formed on the inner surface of the sliding portion instead of the nail, and the plate-shaped fin is configured to be pressed into the femur, and the front wall and There was an artificial knee joint including a femoral side member formed on the inner surface of the rear wall and formed with a plurality of tooth-shaped protrusions having a height of about 1 mm and having a sawtooth shape to enhance the fixing force to the femur.
【0005】[0005]
【発明が解決しようとする課題】しかしながら、上記従
来の人工膝関節において、大腿骨側部材の摺動部の内面
に備えた釘や板状の突起は大腿骨の柔らかく強度の弱い
海綿骨に打ち込まれるよう構成されていたため、これら
によって得られる大腿骨への固定力は補助的な程度のも
のに過ぎず、仮に初期の固定は得られたとしても、体内
での長期間の固定に必要とされる力学的な条件を満たす
ものではなかった。However, in the above-mentioned conventional artificial knee joint, the nail or plate-like projection provided on the inner surface of the sliding portion of the femur side member is driven into the soft and weak cancellous bone of the femur. Therefore, the fixation force to the femur obtained by these is only an auxiliary force, and even if the initial fixation is obtained, it is necessary for long-term fixation in the body. Did not meet the dynamic requirements.
【0006】また、骨切り量を最小限度に留めるという
置換術の原則に照らして考えると、このように大腿骨遠
位部端面のほぼ中央に位置する突起を嵌合するための骨
切りは本来的に余分な骨切りであり、望ましいものでは
なかった。In view of the principle of replacement surgery, which minimizes the amount of osteotomy, the osteotomy for fitting the projection located substantially at the center of the distal end face of the femur as described above is originally used. This was an extra osteotomy and was not desirable.
【0007】[0007]
【発明の目的】本発明の目的は、人工膝関節を構成する
大腿骨側部材の大腿骨への固定力を高めるとともに、そ
の肉厚を小さくするこし、しかるに大腿骨の骨切りが少
量で済む人工膝関節を提供することにある。SUMMARY OF THE INVENTION It is an object of the present invention to increase the fixing force of the femoral side member constituting the artificial knee joint to the femur and to reduce the thickness thereof, thereby reducing the amount of osteotomy of the femur. It is to provide an artificial knee joint.
【0008】[0008]
【課題を解決するための手段】上記課題を解決するめ、
本発明の人工膝関節は大腿骨側部材の前壁及び/又は後
壁の内面の概ね垂直方向に高さ或いは深さ2mm以上、
長さ5mm以上の凸状突起及び/又は凹状溝を形成し
た。In order to solve the above problems,
The knee prosthesis of the present invention has a height or depth of at least 2 mm in a direction substantially perpendicular to the inner surface of the anterior wall and / or posterior wall of the femoral side member,
A convex protrusion and / or a concave groove having a length of 5 mm or more were formed.
【0009】[0009]
【実施例】以下、本発明の実施例を図によって詳しく説
明する。図1は本発明の1例としての人工膝関節Aの斜
視図であり、20は脛骨遠位部を置換する脛骨部材であ
り、1は大腿骨遠位部を置換する大腿骨側部材である。DESCRIPTION OF THE PREFERRED EMBODIMENTS Embodiments of the present invention will be described below in detail with reference to the drawings. FIG. 1 is a perspective view of an artificial knee joint A as an example of the present invention, in which 20 is a tibial member that replaces a distal portion of a tibia, and 1 is a femoral side member that replaces a distal portion of a femur. .
【0010】上記、脛骨部材20の上側は大腿骨部材1
の下側に位置する摺動部4が摺動する摺動面部21とな
っており、また、その下側には脛骨髄腔内に挿入される
べく棒状をなしたステム22が形成されている。The upper side of the tibial member 20 is the femoral member 1
The sliding part 4 located on the lower side is a sliding surface part 21 on which the rod slides, and a stem 22 having a rod shape is formed below the sliding surface part 21 so as to be inserted into the tibial cavity. .
【0011】また、他方の大腿骨部材1は、板状の前壁
2と左右2つの後壁3、3及びこれらを連結し概ね弧状
をなす摺動部4から構成される。The other femoral member 1 is composed of a plate-shaped front wall 2, left and right rear walls 3, 3 and a sliding portion 4 connecting these to form a substantially arcuate shape.
【0012】この大腿骨側部材1の前壁2と摺動部4と
後壁3の外面は、置換する大腿骨の正常状態における関
節摺動面に近似した滑らかな曲面を有し、また、大腿骨
の後方に位置する前後十字靱帯の付着部と干渉する位置
には、上記2つの後壁3と摺動部4の一部を中央で分断
する顆間部5が形成してある。The outer surfaces of the front wall 2, the sliding portion 4 and the rear wall 3 of the femoral side member 1 have a smooth curved surface similar to the joint sliding surface in the normal state of the femur to be replaced. At the position interfering with the attachment portion of the anterior-posterior cruciate ligament located behind the femur, an intercondylar portion 5 is formed which divides the two rear walls 3 and a part of the sliding portion 4 at the center.
【0013】上記前壁内面2aは平坦面をなすととも
に、そのほぼ中央の垂直方向には、骨内に嵌合される凸
状突起として、水平断面半球状で柱状をなした圧接前突
起6が形成してあり、さらに、この圧接前突起6の左右
には、骨の一部を嵌合する凹状溝として上記圧接前突起
6に平行して水平断面半球状の圧接前溝7を2個形成し
ている。The inner surface 2a of the front wall has a flat surface, and in the vertical direction substantially at the center thereof, as a convex protrusion fitted into the bone, a pressing front protrusion 6 having a hemispherical horizontal cross section and a columnar shape is formed. Further, on the left and right of the pre-pressing projection 6, two pre-pressing grooves 7 having a hemispherical horizontal cross section are formed in parallel with the pre-pressing projection 6 as concave grooves for fitting a part of a bone. doing.
【0014】また、上記後壁内面3a、3aは平坦面を
なし、そのほぼ中央の垂直方向には、骨内に嵌合される
凸状突起として、水平断面半球状で柱状をなした圧接後
突起8、8が形成してある。The inner surfaces 3a, 3a of the rear wall are flat surfaces, and in the vertical direction substantially at the center thereof, as a convex protrusion to be fitted into the bone, a columnar shape having a hemispherical horizontal cross section is formed. Protrusions 8, 8 are formed.
【0015】なお、上記圧接前突起6、圧接前溝7の大
きさは、長さ20mm、水平断面の半径が5mmであ
り、また上記圧接後突起8の大きさは、長さ15mm、
水平断面の半径が5mmであり、少なくとも1〜2mm
の圧入しろを確保するようにしてある。The size of the pre-pressing protrusion 6 and the pre-pressing groove 7 is 20 mm in length and the radius of the horizontal cross section is 5 mm. The size of the post-pressing protrusion 8 is 15 mm in length.
The radius of the horizontal section is 5 mm, at least 1-2 mm
The press-fitting margin is secured.
【0016】このように構成される本発明の人工膝関節
Aは、大腿骨部材1を前壁内面2aと、後壁内面3a、
3aに形成した凸状突起(圧接前突起6、圧接後突起
8、8)と凹状溝(圧接前溝7、7)が、上述のように
充分大きな圧入しろをもって、また大きな面積で骨と当
接するように構成したため、大腿骨部材1がこの部分で
骨と強固に嵌合固定する。これによって、大腿骨部材1
内の応力は上記凸状突起と凹状溝の周囲、特に凸状突起
に多く発生するようになり、その分他の部分では応力が
小さくなるため、図1のXーX線断面図である図2、図
1のYーY線断面図である図3において、従来の大腿骨
側部材1′の断面形状を二点鎖線で対比させて示してい
る如く、強度的にも前壁2及び後壁3、3の肉厚を1〜
2mm程度小さくすることができ、その分骨きり量を少
なくすることもできる。In the artificial knee joint A of the present invention configured as described above, the femoral member 1 is connected to the front wall inner surface 2a and the rear wall inner surface 3a.
The convex projections (protrusions 6 before pressing and projections 8 and 8 after pressing) and the concave grooves (grooves 7 and 7 before pressing) formed in 3a have a sufficiently large press fit as described above and a large area to contact the bone. Since the femoral members 1 are configured to be in contact with each other, the femoral member 1 is firmly fitted and fixed to the bone at this portion. Thereby, the femoral component 1
1 are generated around the convex protrusions and the concave grooves, particularly in the convex protrusions, and the stress is reduced in other portions accordingly. 2. As shown in FIG. 3, which is a cross-sectional view taken along the line YY in FIG. 1, the cross-sectional shape of the conventional femur side member 1 'is shown by the two-dot chain line, and the strength of the front wall 2 and the rear wall is also high. The thickness of the walls 3 and 3 is 1 to
It can be reduced by about 2 mm, and the amount of bone can be reduced accordingly.
【0017】なお、大腿骨側部材1に形成する凸状突起
6及び凹状溝7の形状としては、半円柱形状に限られる
ものでなく、図4に示す如く四角柱形状や三角柱形状で
あってもも良い。The shapes of the convex protrusions 6 and the concave grooves 7 formed on the femur side member 1 are not limited to a semi-cylindrical shape, but may be a quadrangular prism shape or a triangular prism shape as shown in FIG. Momo is good.
【0018】また、大腿骨側部材1が大腿骨へ強固に固
定されるには、上記凸状突起及び凹状溝の高さあるいは
深さが2mm以上で長さが5mm以上であることが好ま
しい。他方、深さが2mmより小さく、あるいは長さが
5mmより小さい場合には、仮に初期の固定性が得られ
ても、凸状突起及び凹状溝に過度な応力が発生し、接触
する骨組織が吸収される可能性があるので好ましくな
い。In order for the femoral side member 1 to be firmly fixed to the femur, it is preferable that the height or depth of the convex projections and the concave grooves is 2 mm or more and the length is 5 mm or more. On the other hand, when the depth is smaller than 2 mm or the length is smaller than 5 mm, even if the initial fixation is obtained, excessive stress is generated in the convex projections and the concave grooves, and the bone tissue in contact with the convex projections and the concave grooves is reduced. It is not preferable because it may be absorbed.
【0019】次に、本実施例の人工膝関節Aを構成する
上記大腿骨部材1によって大腿骨遠位部を置換するため
の骨切りについて説明する。図5の斜視図には、上記大
腿骨側部材1を設置するための、骨切りを行った大腿骨
遠位部Fを示し、9は大腿骨側部材1の前壁内面2aが
当接する大腿骨遠位部Fの切除前面、10は大腿骨側部
材1の摺動部内面4aに当接する切除端面、11は大腿
骨側部材1の後壁内面2aに当接する切除後面である。Next, osteotomy for replacing the distal portion of the femur with the above-mentioned femoral member 1 constituting the artificial knee joint A of the present embodiment will be described. The perspective view of FIG. 5 shows a distal portion F of a cut femur for installing the above-mentioned femoral side member 1, and reference numeral 9 denotes a thigh against which the front wall inner surface 2 a of the femoral side member 1 abuts. The resection front face 10 of the bone distal portion F is a resection end face that abuts on the sliding part inner surface 4a of the femoral side member 1, and the resection front face 11 abuts on the rear wall inner surface 2a of the femur side member 1.
【0020】上記切除前面9と切除端面10及び切除端
面10と切除後面11がそれぞれほぼ直角となるよう、
すなわち、切除前面9と切除後面11はほぼ平行となる
よう切除するとともに、上記大腿骨部材1の圧接前溝
7、7に嵌合すべく、これらに対応する切除前面突起1
3、13を、また、上記大腿骨部材1の凸状突起(圧接
前突起6、圧接後突起8)を嵌合すべく、これらに対応
する場所に切除前面溝12及び切除後面溝14、14を
形成しておく。The resection front face 9 and resection end face 10 and the resection front face 10 and post-resection face 11 are substantially perpendicular to each other.
That is, the cut front surface 9 and the cut back surface 11 are cut so as to be substantially parallel to each other, and the cut front protrusions 1 corresponding to the cut front surfaces 7 and 7 of the femoral member 1 are fitted so as to fit into the grooves 7.
In order to fit the protruding projections (protrusions before pressing 6 and post-pressing projections 8) of the femoral member 1, the front and rear resection grooves 12, 14 and 14, 14, Is formed.
【0021】なお、大腿骨遠位部Fの切除前面9の中央
付近、すなわち上記切除前突起6の周囲は骨皮質が最も
残存しやすい部位であり、これにより大腿骨側部材1の
大腿骨への固定力が増大する。The vicinity of the center of the resection front surface 9 of the distal portion F of the femur, that is, the periphery of the pre-resection protrusion 6 is a portion where the bone cortex is most likely to remain. Fixing force increases.
【0022】また、上記切除前面突起13、13は水平
断面において半径5mmの半円であり、他方切除前面溝
12及び切除後面溝14、14は水平断面において半径
4mmの半円であるので、切除前突起13、13は上記
大腿骨部材1に対し1mmの圧入しろを有し、上記大腿
骨部材の凸状突起(圧接前突起6、圧接後突起8)は切
除前溝12及び切除後溝14、14に対し1mmの圧入
しろを有している。The resection front projections 13 and 13 are semicircles having a radius of 5 mm in a horizontal cross section, while the resection front grooves 12 and post-resection grooves 14 and 14 are semicircles having a radius of 4 mm in a horizontal cross section. The anterior projections 13, 13 have a press fit of 1 mm into the femoral component 1, and the convex projections (pre-clamping projection 6, post-clamping projection 8) of the femoral component have a pre-resection groove 12 and a post-resection groove 14, respectively. , 14 with a press-fit margin of 1 mm.
【0023】図6の側面図は、切除前面溝12と切除後
面溝14を形成するため骨切りをする状態の大腿骨遠位
部Fを示し、脛骨Tを屈曲した状態で、大腿骨遠位部F
に、すでに骨切りした切除前面9、切除端面10、切除
後面11に当接するゲージ15を挿着し、このゲージ1
5内に直立する如く設けられたドリルガイド孔16から
ドリルDを作用させ、所定の位置に半円状の溝、すなわ
ち切除前面溝12と切除後面溝14を形成する。FIG. 6 is a side view showing the distal portion F of the femur in a state where an osteotomy is performed to form the resection front groove 12 and the post-resection groove 14, and the tibia T is bent, and the distal portion of the femur is bent. Part F
A gage 15 which comes into contact with the cut front surface 9, the cut end surface 10, and the cut back surface 11 already cut into the bone is inserted into
A drill D is acted on from a drill guide hole 16 provided upright in 5 to form semicircular grooves, ie, a cut front groove 12 and a cut rear groove 14, at predetermined positions.
【0024】この方法によれば、上記ドリルガイド孔1
6に案内されるドリルDによって骨切りするので、±5
0ミクロン程度以内の精度で切除前面溝12と切除後面
溝14を形成することができる。したがって、上記大腿
骨部材1の凸状突起(圧入前突起6及び圧入後突起8、
8)及び凹状溝(圧入前溝7、7)と骨とは、確実に、
1mm程度の圧入しろでもって密着状態に嵌合するた
め、技術的に未熟な術者でも、骨セメントを使用せずに
大腿骨側部材1を十分な固定力で大腿骨に固定すること
ができる。According to this method, the drill guide hole 1
Since the bone is cut by drill D guided to 6, ± 5
The excision front face groove 12 and the post-excision face groove 14 can be formed with an accuracy of about 0 μm or less. Therefore, the convex protrusions (the protrusion 6 before press-fitting and the protrusion 8 after press-fitting,
8) and the concave grooves (grooves 7, 7 before press-fitting) and the bones
Since the fitting is performed in close contact with a press-fit of about 1 mm, even a technically unskilled operator can fix the femoral side member 1 to the femur with a sufficient fixing force without using bone cement. .
【0025】なお、凸状突起及び/または凹状突起の合
計は2個〜10個であることが好ましい。他方、凸状突
起及び/または凹状突起が1個のみの大腿骨部材1内で
は十分な固定力を得ることはできず、また10個以上で
は、必要とされる骨切り量が多くなるすぎるので好まし
くない。It is preferable that the total number of the convex protrusions and / or the concave protrusions is 2 to 10. On the other hand, a sufficient fixing force cannot be obtained in the femoral component 1 having only one convex projection and / or concave projection, and a required amount of osteotomy becomes too large with ten or more convex projections and / or concave projections. Not preferred.
【0026】また、上記凸状突起及び/または凹状突起
は、かならずしも前壁内面2a及び後壁内面3aの両方
に形成する必要はなく、前壁内面2aのみ或いは後壁内
面3aのみに形成しても良い。It is not always necessary to form the convex and / or concave projections on both the front wall inner surface 2a and the rear wall inner surface 3a, but only on the front wall inner surface 2a or only the rear wall inner surface 3a. Is also good.
【0027】[0027]
【発明の効果】上述のように本発明の人工膝関節は、大
腿骨側部材の前壁及び/又は後壁の内面の概ね垂直方向
に高さ或いは深さ2mm以上、長さ5mm以上の凸状突
起及び/又は凹状溝を形成したことにより、大腿骨側部
材を大腿骨に、セメントを用いず、容易かつ強固に固定
することができるとともに、その肉厚を小さくすること
ができるので、骨切り量を最小限に抑えることができ
る。したがって、生体に安全であり、より長期間の使用
に耐える人工膝関節を提供できる。As described above, the knee prosthesis of the present invention has a convexity having a height or depth of at least 2 mm and a length of at least 5 mm in the direction substantially perpendicular to the inner surface of the anterior wall and / or posterior wall of the femoral side member. By forming the protruding protrusions and / or the concave grooves, the femoral side member can be easily and firmly fixed to the femur without using cement, and the thickness can be reduced. The cutting amount can be minimized. Therefore, it is possible to provide an artificial knee joint that is safe for a living body and that can withstand long-term use.
【図1】本発明に係る人工膝関節の斜視図である。FIG. 1 is a perspective view of an artificial knee joint according to the present invention.
【図2】図1のXーX線断面図である。FIG. 2 is a sectional view taken along line XX of FIG.
【図3】図1のYーY線断面図である。FIG. 3 is a sectional view taken along line YY of FIG. 1;
【図4】図1のXーX線断面図である。FIG. 4 is a sectional view taken along line XX of FIG. 1;
【図5】大腿骨遠位部の斜視図である。FIG. 5 is a perspective view of a distal portion of a femur.
【図6】大腿骨遠位部の側面図である。FIG. 6 is a side view of a distal portion of a femur.
A: 人工膝関節 D: ドリル F: 大腿骨遠位部 1: 大腿骨側部材 2: 前壁 2a: 前壁内面 3: 後壁 4: 摺動部 4a: 摺動部内面 5: 顆間部 6: 圧接前突起 7: 圧接前溝 8: 圧接後突起 9: 切除前面 10: 切除端面 11: 切除後面 12: 切除前面溝 13: 切除前面突起 14: 切除後面突起 15: ゲージ 16: ドルリガイド孔 20: 脛骨部材 21: 摺動面部 22: ステム A: Artificial knee joint D: Drill F: Femur distal part 1: Femur side member 2: Anterior wall 2a: Anterior wall inner surface 3: Rear wall 4: Sliding part 4a: Sliding part inner surface 5: Intercondylar part 6: Pre-press projection 7: Pre-press groove 8: Post-press projection 9: Resection front 10: Resection end face 11: Resection rear face 12: Resection front groove 13: Resection front projection 14: Resection rear projection 15: Gauge 16: Dolli guide hole 20 : Tibial member 21: Sliding surface 22: Stem
Claims (1)
び、大腿骨遠位部関節面の前方を置換する前壁と、大腿
骨遠位部関節面後方の内顆側と外顆側を置換する後壁
と、上記前壁と後壁を連結し主たる関節面として機能す
る、概ね弧状の摺動部からなる大腿骨側部材であって、
前壁及び/又は後壁の内面の概ね垂直方向に高さ或いは
深さ2mm以上、長さ5mm以上の凸状突起及び/又は
凹状溝を形成してなる大腿骨側部材、からなる人工膝関
節。1. A tibial member for replacing a distal portion of a tibial bone, an anterior wall for replacing an anterior surface of a joint surface of a distal femur, and medial and lateral condyles behind a joint surface of the distal femur. A rear wall that replaces, and functions as a main joint surface connecting the front wall and the rear wall, a femoral side member comprising a generally arcuate sliding portion,
An artificial knee joint comprising a protruding protrusion and / or concave groove having a height or depth of 2 mm or more and a length of 5 mm or more in a direction substantially perpendicular to the inner surface of the front wall and / or the rear wall. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13036193A JP3113454B2 (en) | 1993-06-01 | 1993-06-01 | Artificial knee joint |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13036193A JP3113454B2 (en) | 1993-06-01 | 1993-06-01 | Artificial knee joint |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH06339491A JPH06339491A (en) | 1994-12-13 |
JP3113454B2 true JP3113454B2 (en) | 2000-11-27 |
Family
ID=15032544
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13036193A Expired - Fee Related JP3113454B2 (en) | 1993-06-01 | 1993-06-01 | Artificial knee joint |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3113454B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112043341A (en) * | 2020-10-12 | 2020-12-08 | 江苏双羊医疗器械有限公司 | Bone raiser special for osteotomy |
-
1993
- 1993-06-01 JP JP13036193A patent/JP3113454B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112043341A (en) * | 2020-10-12 | 2020-12-08 | 江苏双羊医疗器械有限公司 | Bone raiser special for osteotomy |
Also Published As
Publication number | Publication date |
---|---|
JPH06339491A (en) | 1994-12-13 |
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